• 1. Electrochromic ultra-thin films based on cerium polyoxometalate
  Guanggang Gao,Lin Xu,Wenju Wang,Wenjia An,Yunfeng Qiu J. Mater. Chem. 2004 14 2024
• 2. Curcumin associated poly(allylamine hydrochloride)-phosphate self-assembled hierarchically ordered nanocapsules: size dependent investigation on release and DPPH scavenging activity of curcumin
  Mai Mouslmani,Jessica M. Rosenholm,Neeraj Prabhakar,Markus Peurla,Elias Baydoun,Digambara Patra RSC Adv. 2015 5 18740
• 3. The effect of guanidinium functionalization on the structural properties and anion affinity of polyelectrolyte multilayers
  Zheng Cao,Pavlo I. Gordiichuk,Katja Loos,Ernst J. R. Sudh?lter,Louis C. P. M. de Smet Soft Matter 2016 12 1496
• 4. Hybrid poly(allylamine hydrochloride)–graphene oxide microcapsules: preparation, characterization and application in textiles with controlled release behavior
  Zhiqi Zhao,Qiujin Li,Jixian Gong,Zheng Li,Jianfei Zhang Mater. Adv. 2020 1 804
• 5. Photosensitizing properties of hollow microcapsules built by multilayer self-assembly of poly(allylamine hydrochloride) modified with rose Bengal
  Mariana P. Serrano,Matías Rafti,Andrés H. Thomas,Claudio D. Borsarelli RSC Adv. 2019 9 19226

• Solvents and Organic Chemicals Organic Compounds Organic nitrogen compounds Organonitrogen compounds Amines Primary amines
• Solvents and Organic Chemicals Organic Compounds Amines/Sulfonamides
• Catalysts and Inorganic Chemicals Inorganic Compounds Salt

Professional Introduction to Prop-2-en-1-amine Hydrochloride (CAS No. 10017-11-5)

Prop-2-en-1-amine Hydrochloride, chemically known as (E)-2-Aminopropene Hydrochloride, is a significant compound in the field of pharmaceutical and biochemical research. With a CAS number of 10017-11-5, this compound has garnered attention due to its versatile applications and structural properties. This introduction aims to provide a comprehensive overview of Prop-2-en-1-amine Hydrochloride, highlighting its chemical characteristics, potential applications, and recent advancements in research.

The molecular formula of Prop-2-en-1-amine Hydrochloride is C?H?NO·HCl, reflecting its amine functional group and hydrochloride salt form. This structure makes it a valuable intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. The presence of the amine group allows for further functionalization, making it a key building block in medicinal chemistry.

In recent years, Prop-2-en-1-amine Hydrochloride has been explored for its role in the synthesis of various bioactive molecules. Its ability to act as a precursor in the formation of more complex structures has made it indispensable in drug discovery processes. Researchers have leveraged its reactivity to develop novel compounds with potential therapeutic benefits.

One of the most notable applications of Prop-2-en-1-amine Hydrochloride is in the field of protease inhibition. Proteases are enzymes that play crucial roles in various biological processes, and their inhibition is often a target in drug development. Studies have shown that derivatives of Prop-2-en-1-amine can be effective in modulating protease activity, which has implications for treating conditions such as cancer and inflammation.

Moreover, the compound has been investigated for its potential role in neuropharmacology. The amine group's interaction with neurotransmitter systems suggests that Prop-2-en-1-amine Hydrochloride could be used to develop drugs that affect central nervous system function. Recent research has explored its potential as an intermediate in synthesizing compounds that interact with serotonin and dopamine receptors, which are key targets for medications used in treating depression and anxiety disorders.

The synthesis of Prop-2-en-1-amine Hydrochloride typically involves the reaction of propene with ammonia under controlled conditions. This process highlights the compound's importance as a byproduct of industrial chemistry, where it can be efficiently produced on an industrial scale. The hydrochloride salt form enhances its solubility in water, making it more suitable for pharmaceutical formulations.

Recent advancements in computational chemistry have also contributed to the understanding of Prop-2-en-1-amine Hydrochloride's properties. Molecular modeling studies have provided insights into how this compound interacts with biological targets at the molecular level. These insights are crucial for designing more effective drugs with fewer side effects.

In conclusion, Prop-2-en-1-amine Hydrochloride (CAS No. 10017-11-5) is a multifaceted compound with significant applications in pharmaceutical research. Its role as an intermediate in drug synthesis, particularly in protease inhibition and neuropharmacology, underscores its importance. As research continues to uncover new possibilities, this compound is poised to remain a cornerstone in the development of innovative therapeutic agents.

• 30551-89-4(Poly(allylamine))
• 21035-54-1(2-Buten-1-amine (9CI))
• 90387-54-5(Formaldehyde, reaction products with 2-propen-1-amine)
• 58887-05-1(2-Buten-1-amine, (Z)-)
• 56930-04-2(but-2-en-1-amine)
• 1173019-38-9(prop-2-en-1-amine)
• 71550-12-4(Poly(allylamine Hydrochloride))
• 40930-37-8(but-2-ene-1,4-diamine)
• 18231-61-3(2-Butene-1,4-diamine)
• 40794-72-7( )